Table 2. Relative mutation rates of nucleotide i to j per site i for ex-operonic intergenic sites were calculated from singleton SNPs for the two replicatory strands.
from A | T | C | G | Equilibrium frequency | Equilibrium AT skew | ||
Leading | to A | - | 1.79965E-04 | 4.37222E-04 | 6.39046E-04 | 0.2257 | -0.4176 (-0.6792, -0.1522) |
T | 2.34002E-04 | - | 1.67602E-03 | 1.17158E-03 | 0.5493 | ||
C | 6.38189E-05 | 4.72409E-04 | - | 5.32538E-05 | 0.1319 | ||
G | 6.59462E-04 | 4.49913E-05 | 0.00 | - | 0.0931 | ||
Lagging | to A | - | 2.34003E-04 | 1.17158E-03 | 1.67602E-03 | 0.5493 | 0.4176 (0.6792, 0.1522) |
T | 1.79965E-04 | - | 6.39046E-04 | 4.37222E-04 | 0.2257 | ||
C | 4.49913E-05 | 6.59462E-04 | - | 0.00 | 0.0931 | ||
G | 4.72409E-04 | 6.38189E-05 | 5.32538E-05 | - | 0.1319 |
Relative rates were derived from the following leading strand ex-operonic SNP counts, where XY represents a change from nucleotide X to Y: AG 31 GA 12 CG 0 GC 1 GT 22 TA 8 TC 21 TG 2 AC 3 CA 6 AT 11 CT 23. Nucleotide frequencies at compositional equilibrium were derived from the relative mutation rates. Leading and lagging equilibrium AT skews were calculated from equilibrium A and T frequencies. 95% bootstrap intervals are shown in parentheses.